Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060501135
rs1060501135
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
T 0.700 CausalMutation CLINVAR Brugada syndrome 2012. 22789973

2012

dbSNP: rs1060501135
rs1060501135
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
T 0.700 CausalMutation CLINVAR An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing. 20129283

2010